In Situ Characterization and Interfacial Viscoelastic Properties of Pickering Emulsions Stabilized by AIE-Active Modified Alginate and Chitosan Complexes
Abstract:Pickering emulsions stabilized by polysaccharide–polysaccharide
complexes are attractive in many applications. However, how interface
films formed by soft particles affect the stability of Pickering emulsions
has not been well explored. Herein, we designed aggregation-induced
emission (AIE)-active modified alginate (Alg-AIE)/chitosan (CS) polyelectrolyte
complex (Alg-AIE/CS complex) colloidal particles that are used to
stabilize Pickering emulsions. To explore the relationship between
the interface film struct… Show more
“…Compared with the incomplete interfacial film of 0.591 μm in the emulsion stabilized with Ugi-OA alone, a tighter droplet-particle network structure also formed in the continuous phase, making oil droplets more or less captured and fixed . The thickness and stiffness of the interface film could be effectively controlled, which was beneficial to the designability of the HIPPEs …”
Section: Resultsmentioning
confidence: 99%
“…Under the coassembly behavior mediated by Schiff base interaction, the droplets will also form a closer bridge and network structure between the droplets, which is more conducive to the long-term stability of HIPPEs. 57 The interfacial film of particle complexes was further studied by CLSM. As shown in Figure 6, only a thin red ring film fluorescently labeled with rhodamine dye was observed around the oil droplets for the emulsion stabilized with Ugi-OA alone, while a complete and clear particle interface film was formed around the droplet costabilized by NPSs.…”
Section: Appearance and Microscope Photos Of The Emulsion Stabilized ...mentioning
confidence: 99%
“…58 The thickness and stiffness of the interface film could be effectively controlled, which was beneficial to the designability of the HIPPEs. 57 The QCM-D was used to monitor the interaction strength based on the change in resonance frequency (Δf) and energy dissipation (ΔD) caused by the interaction of the Ugi-OA solution with the quartz chips coated with SNs (silica nanoparticles), ASNs. According to the Sauebrey model (the relationship between the oscillation frequency of the oscillating quartz crystal and the mass change), the adsorption quality of the oil−water interface, the thickness and the structural characteristics of the adsorbed layer were analyzed.…”
Section: Appearance and Microscope Photos Of The Emulsion Stabilized ...mentioning
Significant challenges remain in designing sufficient viscoelasticity polysaccharide-based high internal phase Pickering emulsions (HIPPEs) as soft materials for 3D printing. Herein, taking advantage of the interfacial covalent bond interaction between modified alginate (Ugi-OA) dissolved in the aqueous phase and aminated silica nanoparticles (ASNs) dispersed in oil, HIPPEs with printability were obtained. Using multitechniques coupling a conventional rheometer with a quartz crystal microbalance with dissipation monitoring, the correlation between interfacial recognition coassembly on the molecular scale and the stability of whole bulk HIPPEs on the macroscopic scale can be clarified. The results showed that Ugi-OA/ASNs assemblies (NPSs) were strongly retargeted into the oil−water interface due to the specific Schiff base-binding between ASNs and Ugi-OA, further forming thicker and more rigid interfacial films on the microscopic scale compared with that of the Ugi-OA/SNs (bared silica nanoparticles) system. Meanwhile, flexible polysaccharides also formed a 3D network that suppressed the motion of the droplets and particles in the continuous phase, endowing the emulsion with appropriately viscoelasticity to manufacture a sophisticated "snowflake" architecture. In addition, this study opens a novel pathway for the construction of structured all-liquid systems by introducing an interfacial covalent recognition-mediated coassembly strategy, showing promising applications.
“…Compared with the incomplete interfacial film of 0.591 μm in the emulsion stabilized with Ugi-OA alone, a tighter droplet-particle network structure also formed in the continuous phase, making oil droplets more or less captured and fixed . The thickness and stiffness of the interface film could be effectively controlled, which was beneficial to the designability of the HIPPEs …”
Section: Resultsmentioning
confidence: 99%
“…Under the coassembly behavior mediated by Schiff base interaction, the droplets will also form a closer bridge and network structure between the droplets, which is more conducive to the long-term stability of HIPPEs. 57 The interfacial film of particle complexes was further studied by CLSM. As shown in Figure 6, only a thin red ring film fluorescently labeled with rhodamine dye was observed around the oil droplets for the emulsion stabilized with Ugi-OA alone, while a complete and clear particle interface film was formed around the droplet costabilized by NPSs.…”
Section: Appearance and Microscope Photos Of The Emulsion Stabilized ...mentioning
confidence: 99%
“…58 The thickness and stiffness of the interface film could be effectively controlled, which was beneficial to the designability of the HIPPEs. 57 The QCM-D was used to monitor the interaction strength based on the change in resonance frequency (Δf) and energy dissipation (ΔD) caused by the interaction of the Ugi-OA solution with the quartz chips coated with SNs (silica nanoparticles), ASNs. According to the Sauebrey model (the relationship between the oscillation frequency of the oscillating quartz crystal and the mass change), the adsorption quality of the oil−water interface, the thickness and the structural characteristics of the adsorbed layer were analyzed.…”
Section: Appearance and Microscope Photos Of The Emulsion Stabilized ...mentioning
Significant challenges remain in designing sufficient viscoelasticity polysaccharide-based high internal phase Pickering emulsions (HIPPEs) as soft materials for 3D printing. Herein, taking advantage of the interfacial covalent bond interaction between modified alginate (Ugi-OA) dissolved in the aqueous phase and aminated silica nanoparticles (ASNs) dispersed in oil, HIPPEs with printability were obtained. Using multitechniques coupling a conventional rheometer with a quartz crystal microbalance with dissipation monitoring, the correlation between interfacial recognition coassembly on the molecular scale and the stability of whole bulk HIPPEs on the macroscopic scale can be clarified. The results showed that Ugi-OA/ASNs assemblies (NPSs) were strongly retargeted into the oil−water interface due to the specific Schiff base-binding between ASNs and Ugi-OA, further forming thicker and more rigid interfacial films on the microscopic scale compared with that of the Ugi-OA/SNs (bared silica nanoparticles) system. Meanwhile, flexible polysaccharides also formed a 3D network that suppressed the motion of the droplets and particles in the continuous phase, endowing the emulsion with appropriately viscoelasticity to manufacture a sophisticated "snowflake" architecture. In addition, this study opens a novel pathway for the construction of structured all-liquid systems by introducing an interfacial covalent recognition-mediated coassembly strategy, showing promising applications.
“…According to the stabilization mechanism of Pickering emulsion, the solid particles adsorbed at the interface of water and oil irreversibly, which could prevent the aggregation and Ostwald ripening of the droplets. 36 Compared with emulsions stabilized by small-molecule surfactants, SPI-stabilized emulsions own good interfacial and emulsions activities, for which soybean protein was considered to be an effective emulsifier. However, the native SPI showed a highly folded structure with a rough surface under SEM (Figure 1a), which was probably caused by the aggregated particles.…”
Nowadays,
stretchable self-healing hydrogels designed by biomass-based
materials have gathered remarkable attention in numerous frontier
fields such as wound healing, health monitoring issues, and electronic
skin. In this study, soy protein isolate (SPI), a common plant protein,
was cross-linked to nanoparticles (SPI NPs) by Genipin, (Gen) which
was attracted from the native Geniposide. Oil-in-water (O/W) Pickering
emulsion was formed by SPI NPs wrapping the linseed oil, and further
implanted into poly(acrylic acid)/guar gum (PAA/GG)-based self-healing
hydrogels by multiple reversible weak interactions. With the addition
of Pickering emulsion, the hydrogels have achieved a remarkable self-healing
ability (self-healing efficiency could reach 91.6% within 10 h) and
mechanical properties (tensile strength of 0.89 MPa and strain of
853.2%). Therefore, these hydrogels with good reliable durability
have outstanding application prospects in sustainable materials.
“…Compared with traditional organic fluorescent dyes, AIEgens with unique optical properties of large Stokes shift, , strong photobleaching resistance, robust photostability, and low random blinking are more suitable for designing and fabricating the high-performance luminescent labels. In the past few years, various AIEgens embedded nanospheres (AIENPs) with excellent luminescence characteristics have been synthesized via different strategies, including swelling, micro-emulsion, and precipitation polymerization methods . With these AIENPs as signal-amplification labels, several AIENP-based LFIAs have been developed to detect different analytes, including mycotoxins, antibiotics, foodborne pathogens, and biomarkers .…”
Highly luminescent nanospheres have been demonstrated in enhancing the sensitivity of lateral flow immunoassay (LFIA) due to their loading numerous luminescent dyes. However, the photoluminescence intensities of existing luminescent nanospheres are limited due to the aggregation-caused quenching effect. Herein, highly luminescent aggregation-induced emission luminogens embedded nanospheres (AIENPs) with red emission were introduced as signal amplification probes of LFIA for quantitative detection of zearalenone (ZEN). Optical properties of red-emitted AIENPs were compared with time-resolved dyeembedded nanoparticles (TRNPs). Results showed that red-emitted AIENPs have stronger photoluminescence intensity on the nitrocellulose membrane and superior environmental tolerance. Additionally, we benchmarked the performance of AIENP-LFIA against TRNP-LFIA using the same set of antibodies, materials, and strip readers. Results showed that AIENP-LFIA exhibits good dynamic linearity with the ZEN concentration from 0.195 to 6.25 ng/mL, with half competitive inhibitory concentration (IC 50 ) and detection of limit (LOD) at 0.78 and 0.11 ng/mL, respectively. The IC 50 and LOD are 2.07-and 2.36-fold lower than those of TRNP-LFIA. Encouragingly, the precision, accuracy, specificity, practicality, and reliability of this AIENP-LFIA for ZEN quantitation were further characterized. The results verified that the AIENP-LFIA has good practicability for the rapid, sensitive, specific, and accurate quantitative detection of ZEN in corn samples.
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